Review: could Amlodipine Besylate cause Water Retention?


Summary

Water retention is found among people who take Amlodipine Besylate, especially for people who are female, 60+ old , have been taking the drug for 1 - 6 months, also take medication Lasix, and have Hypertension . We study 18,889 people who have side effects while taking Amlodipine besylate from FDA and social media. Among them, 71 have Water retention. Find out below who they are, when they have Water retention and more.

You are not alone

Join a support group for people who take Amlodipine besylate and have Water retention >>>

Personalized health information

On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>

Amlodipine Besylate

Amlodipine besylate has active ingredients of amlodipine besylate. It is often used in high blood pressure. (latest outcomes from Amlodipine besylate 19,664 users)

Water Retention

Water retention has been reported by people with hair loss, joint pain, blood urea increased, urinary tract infection, osteoarthritis (latest reports from 20,586 Water retention patients).

On Aug, 19, 2016

18,889 people reported to have side effects when taking Amlodipine Besylate.
Among them, 71 people (0.38%) have Water Retention


Number of reports submitted per year:

Could Amlodipine besylate cause Water retention?

Time on Amlodipine Besylate when people have Water Retention *:

  • < 1 month: 16.67 %
  • 1 - 6 months: 66.67 %
  • 6 - 12 months: 0.0 %
  • 1 - 2 years: 8.33 %
  • 2 - 5 years: 0.0 %
  • 5 - 10 years: 8.33 %
  • 10+ years: 0.0 %

Gender of people who have Water Retention when taking Amlodipine Besylate *:

  • female: 54.93 %
  • male: 45.07 %

Age of people who have Water Retention when taking Amlodipine Besylate *:

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 7.27 %
  • 20-29: 0.0 %
  • 30-39: 1.82 %
  • 40-49: 10.91 %
  • 50-59: 16.36 %
  • 60+: 63.64 %

Severity if Water Retention when taking Amlodipine Besylate **:

  • least: 33.33 %
  • moderate: 50.0 %
  • severe: 0.0 %
  • most severe: 16.67 %

How people recovered from Water Retention **:

  • while on drug: 0.0 %
  • after off the drug: 0.0 %
  • not yet: 100 %

Top conditions involved for these people *:

  • Hypertension (19 people)
  • Diabetes Mellitus (9 people)
  • Chronic Myeloid Leukaemia (9 people)
  • Angina Pectoris (6 people)
  • Atrial Fibrillation (5 people)

Top co-used drugs for these people *:

  • Lasix (16 people)
  • Furosemide (15 people)
  • Allopurinol (13 people)
  • Metformin Hcl (9 people)
  • Aspirin (8 people)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Water retention when taking Amlodipine besylate?

Browse all side effects of Amlodipine besylate

a b c d e f g h i j k l m n o p q r s t u v w x y z

Drugs that are associated with Water retention

Water retention

Could your condition cause Water retention

Water retention

Can you answer these questions?

More questions for: Amlodipine besylate, Water retention

You may be interested in these reviews

More reviews for: Amlodipine besylate, Water retention


NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.